Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alejandro Garanto

Showing results (21-30 of 82) with videos related to

Pageof 9
Sort By:
Cells|December 23, 2022
Correction of the Splicing Defect Caused by a Recurrent Variant in ABCA4 (c.769-784C>T) That Underlies Stargardt DiseaseTomasz Z Tomkiewicz, Sara E Nieuwenhuis, Frans P M Cremers, et al.
Molecular Genetics and Metabolism|March 1, 2022
Clinical and biochemical footprints of inherited metabolic disorders. VII. Ocular phenotypesAlejandro Garanto, Carlos R Ferreira, Camiel J F Boon, et al.
Stem Cell Research|March 22, 2023
Generation of an induced pluripotent stem cell line carrying a biallelic deletion (SCTCi019-A) in GCDH using CRISPR/Cas9Imke M E Schuurmans, Ka M Wu, Clara D M van Karnebeek, et al.
Lab on a Chip|January 30, 2025
Retina-on-chip: engineering functional <i>in vitro</i> models of the human retina using organ-on-chip technologyTarek Gensheimer, Devin Veerman, Edwin M van Oosten, et al.
Stem Cell Research|August 4, 2023
Generation of an induced pluripotent stem cell line carrying biallelic deletions (SCTCi019-B) in ALDH7A1 using CRISPR/Cas9Imke M E Schuurmans, Ka M Wu, Clara D M van Karnebeek, et al.
Biochimica Et Biophysica Acta|May 3, 2012
Targeted knockdown of Cerkl, a retinal dystrophy gene, causes mild affectation of the retinal ganglion cell layerAlejandro Garanto, Javier Vicente-Tejedor, Marina Riera, et al.
Stem Cell Research|June 27, 2024
Generation of hiPSC lines from four pyridoxine-dependent epilepsy (PDE) patients carrying the variant c.1279G>C in ALDH7A1 in homozygosisImke M E Schuurmans, Clara D M van Karnebeek, Anita D M Hoogendoorn, et al.
Cellular and Molecular Life Sciences : CMLS|August 22, 2021
A look into retinal organoids: methods, analytical techniques, and applicationsTess A V Afanasyeva, Julio C Corral-Serrano, Alejandro Garanto, et al.
Stem Cell Research|June 26, 2024
Generation of hiPSC lines from four glutaric aciduria type I (GA1) patients carrying pathogenic biallelic variants in GCDHImke M E Schuurmans, Clara D M van Karnebeek, Anita D M Hoogendoorn, et al.
Nucleic Acid Therapeutics|May 27, 2024
Antisense Oligonucleotide-Based Rescue of Complex Intronic Splicing Defects in <i>ABCA4</i>Zelia Corradi, Rebekkah J Hitti-Malin, Laura A de Rooij, et al.
Pageof 9

Showing results (21-30 of 82) with videos related to

Sort By:
Pageof 9
Cells|December 23, 2022
Correction of the Splicing Defect Caused by a Recurrent Variant in ABCA4 (c.769-784C>T) That Underlies Stargardt DiseaseTomasz Z Tomkiewicz, Sara E Nieuwenhuis, Frans P M Cremers, et al.
Molecular Genetics and Metabolism|March 1, 2022
Clinical and biochemical footprints of inherited metabolic disorders. VII. Ocular phenotypesAlejandro Garanto, Carlos R Ferreira, Camiel J F Boon, et al.
Stem Cell Research|March 22, 2023
Generation of an induced pluripotent stem cell line carrying a biallelic deletion (SCTCi019-A) in GCDH using CRISPR/Cas9Imke M E Schuurmans, Ka M Wu, Clara D M van Karnebeek, et al.
Lab on a Chip|January 30, 2025
Retina-on-chip: engineering functional <i>in vitro</i> models of the human retina using organ-on-chip technologyTarek Gensheimer, Devin Veerman, Edwin M van Oosten, et al.
Stem Cell Research|August 4, 2023
Generation of an induced pluripotent stem cell line carrying biallelic deletions (SCTCi019-B) in ALDH7A1 using CRISPR/Cas9Imke M E Schuurmans, Ka M Wu, Clara D M van Karnebeek, et al.
Biochimica Et Biophysica Acta|May 3, 2012
Targeted knockdown of Cerkl, a retinal dystrophy gene, causes mild affectation of the retinal ganglion cell layerAlejandro Garanto, Javier Vicente-Tejedor, Marina Riera, et al.
Stem Cell Research|June 27, 2024
Generation of hiPSC lines from four pyridoxine-dependent epilepsy (PDE) patients carrying the variant c.1279G>C in ALDH7A1 in homozygosisImke M E Schuurmans, Clara D M van Karnebeek, Anita D M Hoogendoorn, et al.
Cellular and Molecular Life Sciences : CMLS|August 22, 2021
A look into retinal organoids: methods, analytical techniques, and applicationsTess A V Afanasyeva, Julio C Corral-Serrano, Alejandro Garanto, et al.
Stem Cell Research|June 26, 2024
Generation of hiPSC lines from four glutaric aciduria type I (GA1) patients carrying pathogenic biallelic variants in GCDHImke M E Schuurmans, Clara D M van Karnebeek, Anita D M Hoogendoorn, et al.
Nucleic Acid Therapeutics|May 27, 2024
Antisense Oligonucleotide-Based Rescue of Complex Intronic Splicing Defects in <i>ABCA4</i>Zelia Corradi, Rebekkah J Hitti-Malin, Laura A de Rooij, et al.
Pageof 9